Selected by Anthropic · Startup Program 2026
BioVantageLab exists to make life-science research traceable, connected, and worth building on, now that AI agents produce it faster than anyone can check.
The problem
Science moves forward when results can be checked and built on. In the life sciences, that check already failed often before AI [1][3]. AI agents now run analyses faster than anyone can check them. Newer models still make scientific mistakes [14][15], and the setup around a model, its harness, changes how much of the work holds up [13].
Papers an agent reproduced, same model
42% → 78%Claude Opus 4.5
Only the agent harness changed: one general setup, one built for the task. 45 tasks, December 2025.
Best score on full computational-biology studies
0.48out of 1
Best of 13 frontier models on 20 analyses, August 2026. Agents struggle with data scale, long analysis chains and error recovery.
References GPT-5 invented without web search
51%GPT-5
Claude Sonnet 4: 22%. Gemini 2.5 Pro: 59%. 2026 test of generated citations.
Planted research flaws an auditor caught
55% → 82%paper → logs and code
Reading the run logs and code, not only the AI-written paper, found far more of the flaws.
AI makes research faster. The harness around a model decides how much of that work you can check. Sereh is the harness we are building: every finding keeps its session, file and tool call.
Why we exist
We want a biology lab where any result can be checked against its record, by anyone, in minutes, however fast an agent produced it.
Science has entered the age of AI. An analysis that once took weeks can now run overnight and reach you by morning. That speed could change how fast biology moves.
But a result is only useful if someone can check it. When nobody can say which run, file or model produced a number, speed makes research harder to trust, not easier. We started BioVantageLab to close that gap.
How we solve it
Provenance
Each finding stays linked to the session, the file and the tool call that produced it.
Connection
New work builds on checked findings, so each task does not start from zero.
Transparency
When findings conflict, we flag it. We do not claim to decide what is true.
Control
Your work stays on your computer. Data leaves it only when you pick a cloud model, and you can see which one.
A commitment, in practice
The best streptavidin variant, N49W, scored ΔΔG −1.8 kcal/mol1, about 20× tighter2 binding, with a pose RMSD of 0.9 Å3. A second model rated it 9 / 104. The gain is significant, p < 0.015.
run_07/ddg.log, from the docking session at 02:14.Two of five numbers hold up. The recommendation rested on the other three.
Illustrative example · structure PDB 1STP · values invented
Who we build for
Computational biologists and chemists
Use AI for analysis at full speed, and keep the record you need to defend the result.
Research leads
Check a claim against its source in minutes, not by asking who ran what.
Bio companies
Give partners and investors results with their sources attached.
The tool we are building
Sereh is a research workspace that runs on your own computer. It keeps the record behind each finding and shows you where findings disagree. You work with AI agents and choose the model for each step.





The real app with a sample project · early build, still named Serra inside the app
Mohamed Elrefaiy, founder
I am a chemistry PhD student at UT Austin. I build Sereh so you can stand behind a result, however fast an agent produced it.
Private early access. We will tell you what Sereh records before you install it.